Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
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Biomarker profiling by nuclear magnetic resonance spectroscopy for the prediction of all-cause mortality: an observational study of 17,345 personsGlobal implementation of genomic medicine: We are not aloneLinking a population biobank with national health registries-the estonian experienceGenetic variants linked to education predict longevitySomatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genomeIdentifying Cases of Type 2 Diabetes in Heterogeneous Data Sources: Strategy from the EMIF ProjectThe association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjectsOverview of the BioBank Japan Project: Study design and profilePolymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adultsVariants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan.Smoking-related general and cause-specific mortality in Estonia.The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs.An epidemiological perspective of personalized medicine: the Estonian experience.Dominance genetic variation contributes little to the missing heritability for human complex traits.Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature.How are personality trait and profile agreement related?SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes.MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies.Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells.Copy number variations and cognitive phenotypes in unselected populationsStructural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity.Protocol for the China PEACE (Patient-centered Evaluative Assessment of Cardiac Events) Million Persons Project pilot.Cardiovascular Risk Factors and Ischemic Heart Disease: Is the Confluence of Risk Factors Greater Than the Parts? A Genetic Approach.Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.Autosomal genetic control of human gene expression does not differ across the sexes.Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia.Demographic associations for autoantibodies in disease-free individuals of a European population.The Prevalence of PMM2-CDG in Estonia Based on Population Carrier Frequencies and Diagnosed Patients.Comparing distributions of polygenic risk scores of type 2 diabetes and coronary heart disease within different populations.The Genetic Architecture of Gene Expression in Peripheral Blood.Guidance for the utility of linear models in meta-analysis of genetic association studies of binary phenotypes.Ageing with elegans: a research proposal to map healthspan pathways.Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel.C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis.Metabolites of milk intake: a metabolomic approach in UK twins with findings replicated in two European cohorts.Challenges in understanding common disease.Personal control of privacy and data: Estonian experience.Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations.
P2860
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P2860
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
description
2014 nî lūn-bûn
@nan
2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@ast
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@en
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@nl
type
label
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@ast
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@en
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@nl
prefLabel
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@ast
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@en
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@nl
P2093
P2860
P50
P356
P1476
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.
@en
P2093
Harold Snieder
Helene Alavere
Liis Leitsalu
Mari-Liis Tammesoo
Pauline C Ng
Toomas Haller
P2860
P304
P356
10.1093/IJE/DYT268
P577
2014-02-11T00:00:00Z